PKC beta Proteine (PRKCB)

Human Protein Kinase C, beta (PRKCB) Interaktionspartner

1. our study indicated that PKC alpha and beta appeared coping with oncogenic Ras or mutated Akt to maintain the balance of the homeostasis in cancer cells. Once these PKC isoforms were suppressed, the redox state in the cancer cells was disrupted, which elicited persistent oncogenic stress and subsequent apoptotic crisis.

2. PKC beta would sensitize cervical cancer cells to chemotherapy via reducing the chemotherapy induced autophagy in cancer cells.

3. Loss of PRKCB2 expression is associated with colorectal cancer.

4. significantly different gene expressions of BECN1 and PRKCB between the control and the Alzheimer's disease (AD) groups and of CDKN2A between the control and the preclinical AD groups, are reported.

5. a primary functional variant of PRKCB (rs35015313) was identified by genotype imputation using a phased panel of 1,070 Japanese individuals from a prospective, general population cohort study and subsequent in vitro functional analyses. These results may lead to improved understanding of the disease pathways involved in primary biliary cholangitis.

6. our findings identify PRKCB gene as a novel candidate gene for familial Meniere's Disease (MD )and its expression gradient in supporting cells of the organ of Corti deserves attention, given the role of supporting cells in K(+ )recycling within the endolymph, and its apical turn location may explain the onset of hearing loss at low frequencies in MD

7. Activation of the Pro-Oxidant PKCbetaII-p66Shc (zeige SHC1 Proteine) Signaling Pathway Contributes to Pericyte Dysfunction in Skeletal Muscles of Patients With Diabetes With Critical Limb Ischemia

8. Taken together, these data argue for a complex mechanism of PKC-beta-dependent regulation of SH (zeige POLD3 Proteine)CA (p66) activation invol (zeige SIGLEC1 Proteine)ving Ser(139) and a motif surroun (zeige SIGLEC1 Proteine)ding Ser(213).

9. The study aimed to identify a small set of genetic signatures that may reliably predict the individuals with a high genetic propensity to heroin addiction. A set of 4 genes (JUN (zeige JUN Proteine), CEBPB (zeige CEBPB Proteine), PRKCB, ENO2 (zeige ENO2 Proteine), or CEBPG (zeige CEBPG Proteine)) could predict the diagnosis of heroin addiction with the accuracy rate around 85% in our dataset.

10. Our results provide compelling evidence that glucose-induced PKCalpha (zeige PKCa Proteine)/PKCbeta-mediated inhibition of Kv current in vascular smooth muscle causes an enhanced constrictor response. Inhibition of Kv current causes a significant depolarization of vascular myocytes leading to marked vasoconstriction

Mouse (Murine) Protein Kinase C, beta (PRKCB) Interaktionspartner

1. These results provide a molecular explanation of how initiation of B cell activation (zeige BLNK Proteine) discriminates substrate stiffness through a PKCbeta-mediated FAK (zeige PTK2 Proteine) activation dependent manner.

2. propose that PKCbeta acts to suppress the degradation of FTO (zeige FTO Proteine) protein and reveals the associated role of PKCbeta and FTO (zeige FTO Proteine) in adipogenesis, suggesting a new pathway that affects the development of obesity and metabolic diseases

3. Cytosolic NELL2 specifically interacts with PKC beta isotypes and inhibits PKC beta1 through direct binding to the N-terminal pseudosubstrate domain of PKC beta1.

4. Taken together, these data argue for a complex mechanism of PKCbeta-dependent regulation of p66 (zeige POLD3 Proteine) activation involving Ser (zeige SIGLEC1 Proteine)(139) and a motif surrounding Ser (zeige SIGLEC1 Proteine)(213).

5. Translocation of PKC-betaII from the cytoplasm to membranes is required for phagocytosis of apoptotic cells and is inhibited by soluble beta-glucan

6. repressor of myogenesis; opposes calcineurin function

7. a new mechanism by which PKC-beta activation promotes EC dysfunction caused by the de-regulation of the IL-18 (zeige IL18 Proteine)/IL-18BP (zeige IL18BP Proteine) pathway, leading to increased VCAM-1 (zeige VCAM1 Proteine) expression, monocyte/macrophage adhesion, and accelerated atherosclerotic plaque formation in diabetes

8. These results demonstrate the importance of PKCbetaII in chronic lymphocytic leukemia-like disease progression and suggest a role for PKCalpha (zeige PKCa Proteine) subversion in creating permissive conditions for leukemogenesis.

9. PKCbeta2 inhibition protects mice from gut (zeige GUSB Proteine) ischemia-reperfusion injury by suppressing the adaptor p66(Shc)-mediated oxidative stress and subsequent apoptosis.

10. PKC-alpha (zeige PKCa Proteine) and -betaIotaIota are the predominant isoforms in the developing optic pathway, whereas PKC-epsilon (zeige PRKCE Proteine) is the major form in the chiasmatic neurons.

Cow (Bovine) Protein Kinase C, beta (PRKCB) Interaktionspartner

1. The study identified the serine phosphorylation (p-Ser (zeige SIGLEC1 Proteine)) sites induced by PKC-Beta activation or AGT (zeige AGT Proteine), which inhibits insulin (zeige INS Proteine)-induced p-Tyr (zeige TYR Proteine) sites on IRS2 (zeige IRS2 Proteine) and its signals in endothelial cells.

Pig (Porcine) Protein Kinase C, beta (PRKCB) Interaktionspartner

1. ET-1 (zeige EDN1 Proteine)-mediated myocardial contractile dysfunction during cardioplegia involves activation of protein kinase C beta II.

2. The PKCalpha (zeige PKCa Proteine), PKCbeta1, and PKCbeta2 mRNA levels tended to be lower in ischemia-reperfused than in sham-operated eyes in both the retinal arteries and the neuroretina.

3. Increases in epicardial perivascular adipose tissue leptin (zeige LEP Proteine) exacerbate coronary endothelial dysfunction in MetS via a PKC-beta-dependent pathway.

4. first study to show the expression and cellular localization of PKC beta I in the retina of pigs with development, and these results suggest that PKC beta I, in accordance with PKC alpha (zeige PKCa Proteine), plays important roles in signal transduction pathways in the pig retina with development